Peter Rudd-Clarke

Peter specialises in helping businesses navigate regulatory challenges and liability risks, particularly in the life sciences, healthcare and consumer products sectors. 

Peter advises a range of businesses including medical device companies, software producers, pharmaceutical manufacturers, service providers and producers of lifestyle products.

His regulatory experience includes advising on the regulation of medical devices and consumer products, as well as CE/UKCA marking, clinical trials, regulatory investigations, the application of industry codes and ongoing compliance matters.

The litigation and risk management side to Peter’s practice involves defending manufacturers of complex products against liability claims, often across multiple jurisdictions; as well as advising clients on product recalls and corrective actions. 

Peter is ranked in the Legal 500.

  • Next: 8-9 Jul 2024 Classroom
  • Also: 20-21 Nov 2024 Live online

Drafting Commercial Contracts for the Pharmaceutical Industry

Live online, Classroom

A two-day practical and interactive seminar focusing on current contract drafting, negotiating, best practice and related issues within the pharmaceutical, biotech and life sciences sectors.

  • 12 CPD hours Focused
  • Presented by Peter Rudd-Clarke